Taiwan FDA registration fc8bcf237c77706156a87a938a201706

"Biosen Webster" Webster automatically identifies bidirectional flexible coronary sinus electrophysiological catheters

TW: “百歐森偉伯斯特”偉伯司特自動辨識雙向可彎式冠狀靜脈竇電生理導管
Taiwan flagTaiwan·Risk Class 2·Biosense Webster, Inc.·Registered Jul 16, 2012 – Jul 16, 2027Active
Registration details
Analysis ID
fc8bcf237c77706156a87a938a201706
Customs Code
DHA00602377303
Company information
Manufacturer Country
Mexico;;United States
Authorized Representative
JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.1220 電極記錄導管或電極記錄探頭
Import Information
import
Dates and status
Registration Date
Jul 16, 2012
Expiry Date
Jul 16, 2027
Cancellation Date
Oct 24, 2024
About this record

Access comprehensive regulatory information for "Biosen Webster" Webster automatically identifies bidirectional flexible coronary sinus electrophysiological catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fc8bcf237c77706156a87a938a201706 and manufactured by Biosense Webster, Inc.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..

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